Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant

MONDO:0013655

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the GRIN1 gene.

Also known as: GRIN1 autosomal dominant non-syndromic intellectual disability, MRD8, NDHMSD, autosomal dominant intellectual disability 8, autosomal dominant non-syndromic intellectual disability caused by mutation in GRIN1, intellectual disability, autosomal dominant 8, intellectual disability, autosomal dominant type 8, mental retardation, autosomal dominant 8

1 clinical trial for this condition and its sub-types, 0 tagged with Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Intellectual disability, autosomal dominant (23) ↑ GRIN1-related complex neurodevelopmental disorder (0)

Including sub-types (1) Tagged with Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.